Abstract

Spinal cord injury (SCI) is a devasting condition with no reliable treatment. Spina bifida is the most common cause of congenital SCI. Cell-based therapies using mesenchymal stem/stromal cells (MSCS) have been largely utilized in SCI. Several clinical trials for acquired SCI use adult tissue-derived MSC sources, including bone-marrow, adipose, and umbilical cord tissues. The first stem/stromal cell clinical trial for spina bifida is currently underway (NCT04652908). The trial uses early gestational placental-derived mesenchymal stem/stromal cells (PMSCs) during the fetal repair of myelomeningocele. PMSCs have been shown to exhibit unique neuroprotective, angiogenic, and antioxidant properties, all which are promising applications for SCI. This review will summarize the unique properties and current applications of PMSCs and discuss their therapeutic role for acquired SCI.

Highlights

  • Cell-based therapies for spinal cord injury (SCI) have been investigated in preclinical and clinical trials with limited success [1,2]

  • Cytokine arrays and single cell analysis have studied the secretome of placental early gestational chorionic villusderived mesenchymal stem/stromal cells (MSCs) (PMSCs), which is key to understanding the differences between various MSCs

  • Proteomic analysis of PMSC extracellular vesicles (EVs) revealed the presence of several proteins and RNAs involved in neuronal survival

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Summary

A Novel Source of Therapy for Congenital and Acquired Spinal

Edwin S Kulubya 1,2 , Kaitlin Clark 1,3 , Dake Hao 1,3 , Sabrina Lazar 1,3 , Arash Ghaffari-Rafi 2 , Tejas Karnati 2 , Julius Okudu Ebinu 2 , Marike Zwienenberg 2 , Diana L Farmer 1,3 and Aijun Wang 1,3,4, *.

Introduction
Spinal Cord Injury Pathogenesis
Isolation and Culture
PMSC Characterization
PMSC-Secretome—Free Proteins
Neuroprotection
Immunomodulation
Myelin Regeneration
Angiogenesis
Delivery
Surface Modification
Cargo Loading
Congenital SCI
Acquired SCI
Active
Findings
Conclusions
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